A randomized trial of ultrasound-guided peripheral IV catheter placement in difficult access patients using a guidewire approach

被引:6
|
作者
Cochrane, Haley K. [1 ]
Henwood, Patricia C. [2 ]
Platz, Elke [2 ]
Koskenoja, Viktoria [3 ]
Landry, Adaira [2 ]
Frasure, Sarah E. [4 ]
Rempell, Joshua S. [5 ]
Hoyler, Janet [2 ]
Baker, Olesya [2 ]
Kimberly, Heidi H. [2 ]
机构
[1] Univ Saskatchewan, Dept Emergency Med, 2646 Royal Univ Hosp,103 Hosp Dr, Saskatoon, SK S7N 0W8, Canada
[2] Brigham & Womens Hosp, Dept Emergency Med, 75 Francis St, Boston, MA 02115 USA
[3] UP Hlth Syst Marquette, Dept Emergency Med, 580 W Coll Ave, Marquette, MI 49855 USA
[4] George Washington Univ Hosp, Dept Emergency Med, 2120 L St NW,Suite 450, Washington, DC 20037 USA
[5] Cooper Univ Hosp, Dept Emergency Med, 1 Cooper Plaza, Camden, NJ 08103 USA
来源
关键词
Ultrasound; Catheterization peripheral; Vascular access devices; VENOUS ACCESS; INTRAVENOUS ACCESS; ULTRASONOGRAPHY; CANNULATION; GUIDANCE; RISK; VEIN;
D O I
10.1016/j.ajem.2019.07.022
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Objective: The purpose of this pilot study was to investigate whether use of a guidewire improves successful placement of ultrasound-guided peripheral IVs (PIV) in difficult intravenous access patients in the emergency department (ED). Methods: This was an unblinded, prospective, randomized trial performed by emergency medicine (EM) clinicians at a single academic ED. Eligible participants were randomized to ultrasound-guided PIV placement with or without the use of a guidewire. PIV access was obtained using the Accucath (TM) 20 gauge x 5.7 cm catheters by way of deployment or non-deployment of the guidewire. Primary outcome measure was first-pass success rate and secondary outcomes included number of attempts, complication rates, and clinician reported ease of insertion. Results: Seventy patients were enrolled and 69 were included in the final analysis. Thirty-four participants were randomized to use of guidewire and 35 to no guidewire. First-pass success rates were similar with and without guidewire use, 47.1% vs. 45.7%, (p = 0.9). There were no differences found in median number of attempts between the two techniques, 2 (IQR 1-2) vs 2 (IQR 1-2), (p = 0.60). The complication rates were similar, 15% vs. 29% (p = 0.25). Clinicians reported no difference in ease of insertion between methods on a 5-point Likert Scale, mean 2.6 vs 2.7 (p = 0.76). Discussion: In this pilot study comparing ultrasound-guided PIV placement in ED patients using an integrated guidewire versus no guidewire, there was no significant difference in first-pass success, number of attempts, or complication rates. This study provides preliminary data for further investigations. (C) 2019 Elsevier Inc. All rights reserved.
引用
收藏
页码:122 / 126
页数:5
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